Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

A Study of Norepinephrine in Patients With Congenital Insensitivity to Pain and Anhidrosis

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02624310
Recruitment Status : Withdrawn
First Posted : December 8, 2015
Last Update Posted : September 12, 2016
Sponsor:
Information provided by (Responsible Party):
NYU Langone Health

Tracking Information
First Submitted Date  ICMJE September 30, 2014
First Posted Date  ICMJE December 8, 2015
Last Update Posted Date September 12, 2016
Study Start Date  ICMJE January 2016
Estimated Primary Completion Date January 2019   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: December 3, 2015)
Incidence of Treatment-Emergent Adverse Events [ Time Frame: 8 weeks ]
Safety and tolerability will be assessed using general physical and neurological examinations, vital signs including blood pressure and heart rate, temperature and body weight, blood chemistries including serum creatinine, electrolytes, transaminases and liver function tests, 12 lead electrocardiograms and adverse events monitoring.
Original Primary Outcome Measures  ICMJE Same as current
Change History Complete list of historical versions of study NCT02624310 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures  ICMJE Not Provided
Original Secondary Outcome Measures  ICMJE Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE A Study of Norepinephrine in Patients With Congenital Insensitivity to Pain and Anhidrosis
Official Title  ICMJE A Phase II, Randomized, Double Blind, Cross-over, Placebo-controlled Study on Norepinephrine Replenishment Therapy Using L-DOPS in Congenital Insensitivity to Pain With Anhidrosis Patients
Brief Summary

The aim of this study is to increase norepinephrine levels in a population of young adults where NE levels are very low or undetectable. In order to achieve this, the optimal dose will be determined in a titration step. In the titration step, different doses of L-DOPS will be tested in order to find the optimal and safest dose suitable for each individual enrolled in the study. Because L-DOPS has never been used in the US in children or young adults, with this titration step investigators will also determine the safest dose for this population.

Currently, L-DOPS is being used in our center to treat othostatic hypotension in autonomic failure. The titration step for this study starts with the dose of 100 mg and increases in an escalating manner up to a maximum of 600 mg a day (see investigational brochure attached).

L-DOPS has been developed in capsules for oral used and all the previous safety data has been performed using this route. Oral route is the one that will used during study.

Carbidopa is well tolerated, safe in children and it has been used in this population in the US without severe adverse effects.

Detailed Description

CIPA patient do have very low or undetectable levels of norepinephrine in plasma and also have significant cognitive and behavioral problems. The aim of this project is to increase NE levels in brain and evaluate if this increase improve cognitive cognition or behavior.

Both drugs from the study have never been used in CIPA patients before, it is therefore very important to evaluate safety and tolerability of L-DOPS and carbidopa in this population.

Even if NE levels are very low in plasma of CIPA subjects, it is not know if NE levels are also low in central nervous system. It is very likely that this is also the case, however, levels of NE in brain will be checked in one CIPA subject as a prof of concept.

Study overview: Patients with CIPA will be screened and enrolled (visit 1) into part 1 of the pilot trial. Safety parameters including, adverse events, blood chemistries for renal and liver function testing, 12 lead electrocardiogram, temperature, weight and blood pressure (supine, seated and standing), non-verbal intelligence and behavior test, 24 hour urinary catecholamine excretion and plasma dopamine levels will be measured at baseline.

The patients will enter an open-label dose titration phase (visit 2a,b,c,d,e,f) during which adverse events will be continuously monitored. After reaching a dose the 100 mg/day dose, patients will be questioned about adverse events and have their blood pressure (supine, sitting and standing) measured. If no adverse events or abnormalities are detected patients will continue the dose titration. Safety assessments will be repeated and safety bloods obtained when the patient reaches the maximum tolerated dose.

After completion of the dose titration, patients who are able to tolerate L-DOPS will enter into a second open-label dose titration phase where carbidopa will be titrated (visit 3a,b,c,d,e,f). A period of two weeks will be allowed to washout the L-DOPS before starting with the carbidopa titration.

Carbidopa have been previously used in clinical studies in children, young adults and adults in our group and no adverse effects have been reported. There is no reason to think that carbidopa may be unsafe in CIPA patients, however, the aim of these titration step is to check safety and tolerability of the drug in this population. Subjects will receive a dose of 100 mg/day and will be questioned about adverse events and have their blood pressure (supine, sitting and standing) measured. If no adverse events or abnormalities are detected patients will continue the dose titration. In the following steps, the doses of carbidopa will be increased 100 mg daily up to a total of 600 mg/day. Safety assessments will be repeated and safety bloods obtained when the patient reaches a total daily dose of 600 mg/day.

In the final phase of the titration, both L-DOPS and carbidopa will be administered (visit 4a,b,c,d,e). The starting dose of L-DOPS will be the maximum tolerated dose during the L-DOPS titration step. The dose of carbidopa that will be administered with L-DOPS will be the maximum tolerated dose. L-DOPS will be increase in 100 mg/day up to 600 mg/day, unless any adverse affect is observed and then the titration will stop at that dose of L-DOPS. The dose of carbidopa will be the maximum tolerated during the titration and will not be increased.

After reaching the maximum L-DOPS/carbidopa tolerated dose, patients will be questioned about adverse events with the medication and have their blood pressure (supine, sitting and standing) measured. After the safety evaluation if no adverse events or abnormalities are observed in the patients will continue with the study. A period of two weeks will be allowed to washout the L-DOPS/carbidopa before starting with placebo-controlled double-blind cross over phase.

Patients who successfully complete titration will proceed to the randomized placebo control phase. Before proceeding to this part, researcher will review of safety data from the titration. Patients will be randomized in a double-blind fashion, to receive either L-DOPS/carbidopa or matching placebo. Patients will take the medication for 4 weeks.

After 4 weeks, 24 urinary catecholamine excretion, plasma dopamine levels, behavior scores, safety parameters and adverse events will be measured (visit 5), before patients are crossed over (visit 6). A similar dose withdrawal scheme will be implemented to prevent adverse effects from acute withdrawal. Patients will be followed for a further 4-weeks. After completion of the cross over period, patients will undergo final evaluation (visit 7) during which safety and efficacy measures will be repeated. To conclude the study, 2 weeks after completing the pilot-trial, patients will receive a follow up phone call to monitor any adverse events.

All necessary safety information will be reported to the FDA in accordance with 312.32 IND safety reports as outlined in Title 21 Food and Drugs.

Study Type  ICMJE Interventional
Study Phase  ICMJE Phase 2
Study Design  ICMJE Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
Condition  ICMJE HSAN Type IV
Intervention  ICMJE
  • Drug: Droxidopa (L-DOPS)
    Patients will be given their initial 100 mg of L-DOPS (visit 2a). The dose of L-DOPS will be increased in escalation in the following visits. Each day the dose will be increased 100 mg. The escalating doses of L-DOPS will be 200 mg (visit 2b), 300 mg (visit 2c), 400 mg (visit 2d), 500 mg (visit 2e) and 600 mg (visit 2f). Following this titration step, L-DOPS will be withdrawn from the subjects for a minimum of two weeks, when the subject will return for visit 3.Visit 3a,b,c,d,e,f: Carbidopa open-label dose titration. This titration step will be similar than L-DOPS titration. Carbidopa starting dose will be 100 mg (visit 3a) and will be increased 100 mg each visit up to a maximum of 600 mg (visit 3f). Following carbidopa titration step, patients will be withdrawn from the drug for minimum of two weeks, then the subject will return for the next titration step (visit 4).
    Other Name: Northera
  • Drug: Placebo
Study Arms  ICMJE
  • Experimental: Droxidopa First, Placebo Second
    Participants in this arm will receive droxidopa first, then cross over and receive placebo
    Interventions:
    • Drug: Droxidopa (L-DOPS)
    • Drug: Placebo
  • Experimental: Placebo First, Droxidopa Second
    Participants in this arm will receive placebo first, then cross over and receive droxidopa
    Interventions:
    • Drug: Droxidopa (L-DOPS)
    • Drug: Placebo
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Withdrawn
Actual Enrollment  ICMJE
 (submitted: March 7, 2016)
0
Original Estimated Enrollment  ICMJE
 (submitted: December 3, 2015)
10
Estimated Study Completion Date  ICMJE January 2019
Estimated Primary Completion Date January 2019   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  • Male or female 15 years old or older
  • Patient carrying the genetic mutation for the NTRK1 gene
  • Patients (or guardian if patient it is underage) have signed a written consent to participate in the study after being fully informed about the procedure of the study and their right to withdraw at anytime during it.

Exclusion Criteria:

  • Patients taking amphetamines, norepinephrine reuptake inhibitors.
  • Patients taking any medication that can interact with the study drug L- DOPS.
  • Patients with previous severe hypertension (systolic blood pressure >170 mmHg)
  • Patients with arrhythmias or any other cardiac condition.
  • Women who are pregnant or breast feeding
  • Have a renal or hepatic disease
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 15 Years and older   (Child, Adult, Older Adult)
Accepts Healthy Volunteers  ICMJE No
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE Not Provided
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT02624310
Other Study ID Numbers  ICMJE 14-01774
Has Data Monitoring Committee No
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement  ICMJE Not Provided
Responsible Party NYU Langone Health
Study Sponsor  ICMJE NYU Langone Health
Collaborators  ICMJE Not Provided
Investigators  ICMJE Not Provided
PRS Account NYU Langone Health
Verification Date September 2016

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP